A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759784



Internal ID9981929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:120876200..121142359hg38UCSC Ensembl
Innerchr10:122635712..122901873hg19UCSC Ensembl
Innerchr10:122625702..122891863hg18UCSC Ensembl
Innerchr10:122625702..122891863hg17UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg38266160
hg19266162
hg18266162
hg17266162
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758241
SamplesNA19099, NA19173, NA18852
Known GenesMIR5694, WDR11
MethodBAC aCGH
AnalysisArray images were acquired using an Agilent laser scanner (Agilent Technologies, UK). Fluorescence intensities and log2 ratio values were extracted using Bluefuse software (Bluegnome Ltd).
PlatformAgilent
Comments
ReferenceRedon_et_al_2006
Pubmed ID17122850
Accession Number(s)esv2759784
Frequency
Sample Size270
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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